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Dynamic gene expression and growth underlie cell-to-cell heterogeneity in Escherichia coli stress response
Cell-to-cell heterogeneity in gene expression and growth can have critical functional consequences, such as determining whether individual bacteria survive or die following stress. Although phenotypic variability is well documented, the dynamics that underlie it are often unknown. This information i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168488/ https://www.ncbi.nlm.nih.gov/pubmed/35344432 http://dx.doi.org/10.1073/pnas.2115032119 |
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author | Sampaio, Nadia M. V. Blassick, Caroline M. Andreani, Virgile Lugagne, Jean-Baptiste Dunlop, Mary J. |
author_facet | Sampaio, Nadia M. V. Blassick, Caroline M. Andreani, Virgile Lugagne, Jean-Baptiste Dunlop, Mary J. |
author_sort | Sampaio, Nadia M. V. |
collection | PubMed |
description | Cell-to-cell heterogeneity in gene expression and growth can have critical functional consequences, such as determining whether individual bacteria survive or die following stress. Although phenotypic variability is well documented, the dynamics that underlie it are often unknown. This information is important because dramatically different outcomes can arise from gradual versus rapid changes in expression and growth. Using single-cell time-lapse microscopy, we measured the temporal expression of a suite of stress-response reporters in Escherichia coli, while simultaneously monitoring growth rate. In conditions without stress, we found several examples of pulsatile expression. Single-cell growth rates were often anticorrelated with reporter levels, with changes in growth preceding changes in expression. These dynamics have functional consequences, which we demonstrate by measuring survival after challenging cells with the antibiotic ciprofloxacin. Our results suggest that fluctuations in both gene expression and growth dynamics in stress-response networks have direct consequences on survival. |
format | Online Article Text |
id | pubmed-9168488 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-91684882022-09-28 Dynamic gene expression and growth underlie cell-to-cell heterogeneity in Escherichia coli stress response Sampaio, Nadia M. V. Blassick, Caroline M. Andreani, Virgile Lugagne, Jean-Baptiste Dunlop, Mary J. Proc Natl Acad Sci U S A Biological Sciences Cell-to-cell heterogeneity in gene expression and growth can have critical functional consequences, such as determining whether individual bacteria survive or die following stress. Although phenotypic variability is well documented, the dynamics that underlie it are often unknown. This information is important because dramatically different outcomes can arise from gradual versus rapid changes in expression and growth. Using single-cell time-lapse microscopy, we measured the temporal expression of a suite of stress-response reporters in Escherichia coli, while simultaneously monitoring growth rate. In conditions without stress, we found several examples of pulsatile expression. Single-cell growth rates were often anticorrelated with reporter levels, with changes in growth preceding changes in expression. These dynamics have functional consequences, which we demonstrate by measuring survival after challenging cells with the antibiotic ciprofloxacin. Our results suggest that fluctuations in both gene expression and growth dynamics in stress-response networks have direct consequences on survival. National Academy of Sciences 2022-03-28 2022-04-05 /pmc/articles/PMC9168488/ /pubmed/35344432 http://dx.doi.org/10.1073/pnas.2115032119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Sampaio, Nadia M. V. Blassick, Caroline M. Andreani, Virgile Lugagne, Jean-Baptiste Dunlop, Mary J. Dynamic gene expression and growth underlie cell-to-cell heterogeneity in Escherichia coli stress response |
title | Dynamic gene expression and growth underlie cell-to-cell heterogeneity in Escherichia coli stress response |
title_full | Dynamic gene expression and growth underlie cell-to-cell heterogeneity in Escherichia coli stress response |
title_fullStr | Dynamic gene expression and growth underlie cell-to-cell heterogeneity in Escherichia coli stress response |
title_full_unstemmed | Dynamic gene expression and growth underlie cell-to-cell heterogeneity in Escherichia coli stress response |
title_short | Dynamic gene expression and growth underlie cell-to-cell heterogeneity in Escherichia coli stress response |
title_sort | dynamic gene expression and growth underlie cell-to-cell heterogeneity in escherichia coli stress response |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168488/ https://www.ncbi.nlm.nih.gov/pubmed/35344432 http://dx.doi.org/10.1073/pnas.2115032119 |
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